Aggressive Disease Treatment Patterns and CtDNA HRR evaluatiON in High-volume metastatiC hORmone-sensitive Prostate Cancer in Russian FeDeration

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age18+
SponsorAstraZeneca

About this trial

A multicentre observational study on treatment patterns and ctDNA HRR evaluation in aggressive high-volume metastatic hormone-sensitive prostate cancer in Russian Federation

Eligibility criteria

Qualifiers

Male patients aged ≥ 18 years old;

Signed ICF, including consent for blood samples ctDNA and ctDNA-based HRRm testing;

Metastatic hormone-sensitive prostate cancer (mHSPC) (de novo or progressed from earlier stages);

High-aggressive disease (Gleason 8-10);

Disqualifiers

Participation in any interventional trial since the mPC diagnosis.

Progression to mCRPC.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Sponsors and collaborators